Cas 1059682-06-2,5-(tert-butyloxycarbonyl)-1-(4-nitrophenyl)-1,4-dihydro-5H-[1,2,3]triazolo[4,5-c][1,5]naphthyridine

1059682-06-2

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Basic information

Product Name: 5-(tert-butyloxycarbonyl)-1-(4-nitrophenyl)-1,4-dihydro-5H-[1,2,3]triazolo[4,5-c][1,5]naphthyridine
Synonyms: 5-(tert-butyloxycarbonyl)-1-(4-nitrophenyl)-1,4-dihydro-5H-[1,2,3]triazolo[4,5-c][1,5]naphthyridine
CAS NO:1059682-06-2
Molecular Formula:
Molecular Weight: 394.39
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-(tert-butyloxycarbonyl)-1-(4-nitrophenyl)-1,4-dihydro-5H-[1,2,3]triazolo[4,5-c][1,5]naphthyridine(CAS DataBase Reference)
NIST Chemistry Reference: 5-(tert-butyloxycarbonyl)-1-(4-nitrophenyl)-1,4-dihydro-5H-[1,2,3]triazolo[4,5-c][1,5]naphthyridine(1059682-06-2)
EPA Substance Registry System: 5-(tert-butyloxycarbonyl)-1-(4-nitrophenyl)-1,4-dihydro-5H-[1,2,3]triazolo[4,5-c][1,5]naphthyridine(1059682-06-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1059682-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1059682-06-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,9,6,8 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1059682-06:
(9*1)+(8*0)+(7*5)+(6*9)+(5*6)+(4*8)+(3*2)+(2*0)+(1*6)=172
172 % 10 = 2
So 1059682-06-2 is a valid CAS Registry Number.

1059682-06-2Upstream product

1059682-28-8 N-(2-bromopyridyl)-N-tert-butoxycarbonyl-(1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methanamine

1059682-06-2Downstream Products

1059682-06-2Relevant academic research and scientific papers

N,N-Disubstituted propargylamines as tools in the sequential 1,3-dipolar cycloaddition/arylation processes to the formation of polyheterocyclic systems

Basolo, Luca,Beccalli, Egle M.,Borsini, Elena,Broggini, Gianluigi,Pellegrino, Sara

, p. 8182 - 8187 (2008/12/21)

Starting from N,N-disubstituted propargylamines, through a one-pot sequential 1,3-dipolar cycloaddition/Pd-catalyzed arylation, polyheterocyclic systems were obtained in only one step. The outcome of the cycloadditions, performed with 1,3-dipoles nitrilox

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